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Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting immunostaining in relation to complex human pathologies.

Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding. Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".

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OPN1MW / GCP Antibody (aa21‑50) LS‑C163125
GCP antibody LS-C163125 is an unconjugated rabbit polyclonal antibody to human GCP (OPN1MW). Validated for Flow and WB.
Catalog
Size
Price
LS-C163125-400
400 µl
$305

Popular OPN1MW / GCP Products

Antibody
Species: Human
Applications: Western blot, Flow Cytometry, ELISA
Immunofluorescence staining of HepG2 cells diluted at 1:66, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C.The Secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).
Species: Human
Applications: Immunofluorescence, Western blot, ELISA
Antibody
Species: Human
Applications: Western blot, Flow Cytometry, ELISA
Antibody
Species: Human
Applications: Western blot, Flow Cytometry, ELISA
Antibody
Species: Human
Applications: Western blot, Flow Cytometry, ELISA

Product Description

GCP antibody LS-C163125 is an unconjugated rabbit polyclonal antibody to human GCP (OPN1MW). Validated for Flow and WB.

Specifications

Target
Human OPN1MW / GCP
Synonyms
OPN1MW, CBD, CBBM, COD5, Color blindness, deutan, Cone dystrophy 5 (X-linked), Deutan, Green/red, GCP, Green cone pigment, Green photoreceptor pigment, GOP, Green opsin, OPN1MW1, Photopigment apoprotein, Medium-wave-sensitive opsin 1, Green-sensitive opsin
Host
Rabbit
Reactivity
Human (tested or 100% immunogen sequence identity)
Predicted
Rat, Chicken, Xenopus (at least 90% immunogen sequence identity)
Clonality
Polyclonal
Conjugations
Unconjugated
Purification
Protein A purified
Modifications
Unmodified
Applications
  • Western blot (1:1000)
  • Flow Cytometry (1:10 - 1:50)
Blocking Peptide
LS-E7642 - Lyophilized - 100 µg - $145.00
Immunizing peptide used to generate LS-C163125. Useful for pre-absorption and neutralization of the antibody's antigen binding site.
Epitope
aa21-50
Specificity
This OPN1MW antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 21-50 amino acids from the N-terminal region of human OPN1MW.
Presentation
PBS, 0.09% Sodium Azide
Storage
Maintain refrigerated at 2°C to 8°C for up to 6 months. For long term storage store at -20°C.
Restrictions
For research use only.
About OPN1MW / GCP
OPN1MW / GCP is for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. P04001 NM_000513 NP_000504.1


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Images

Western blot

Western blot of OPN1MW Antibody in HepG2 cell line lysates (35 ug/lane). OPN1MW (arrow) was detected using the purified antibody.
Western blot of OPN1MW Antibody in HepG2 cell line lysates (35 ug/lane). OPN1MW (arrow) was detected using the purified antibody.

Flow Cytometry

OPN1MW Antibody flow cytometry of HepG2 K10cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
OPN1MW Antibody flow cytometry of HepG2 K10cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Western blot

Western blot of OPN1MW Antibody in HepG2 cell line lysates (35 ug/lane). OPN1MW (arrow) was detected using the purified antibody.
Western blot of OPN1MW Antibody in HepG2 cell line lysates (35 ug/lane). OPN1MW (arrow) was detected using the purified antibody.

Flow Cytometry

OPN1MW Antibody flow cytometry of HepG2 K10cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
OPN1MW Antibody flow cytometry of HepG2 K10cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Western blot

Western blot of OPN1MW Antibody in HepG2 cell line lysates (35 ug/lane). OPN1MW (arrow) was detected using the purified antibody.
Western blot of OPN1MW Antibody in HepG2 cell line lysates (35 ug/lane). OPN1MW (arrow) was detected using the purified antibody.

Flow Cytometry

OPN1MW Antibody flow cytometry of HepG2 K10cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
OPN1MW Antibody flow cytometry of HepG2 K10cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Western blot

Western blot of OPN1MW Antibody in HepG2 cell line lysates (35 ug/lane). OPN1MW (arrow) was detected using the purified antibody.
Western blot of OPN1MW Antibody in HepG2 cell line lysates (35 ug/lane). OPN1MW (arrow) was detected using the purified antibody.

Flow Cytometry

OPN1MW Antibody flow cytometry of HepG2 K10cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
OPN1MW Antibody flow cytometry of HepG2 K10cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Requested From: United States
Date Requested: 11/14/2018

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